JP2009541268A5 - - Google Patents
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- JP2009541268A5 JP2009541268A5 JP2009515885A JP2009515885A JP2009541268A5 JP 2009541268 A5 JP2009541268 A5 JP 2009541268A5 JP 2009515885 A JP2009515885 A JP 2009515885A JP 2009515885 A JP2009515885 A JP 2009515885A JP 2009541268 A5 JP2009541268 A5 JP 2009541268A5
- Authority
- JP
- Japan
- Prior art keywords
- pyrazin
- alkyl
- indol
- amino
- amine
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
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- 125000000217 alkyl group Chemical group 0.000 claims 75
- 150000001875 compounds Chemical class 0.000 claims 23
- 125000000623 heterocyclic group Chemical group 0.000 claims 23
- -1 aminocarbonylphenyl Chemical group 0.000 claims 16
- 125000003545 alkoxy group Chemical group 0.000 claims 12
- 150000003839 salts Chemical class 0.000 claims 11
- 125000001424 substituent group Chemical group 0.000 claims 10
- 229910052739 hydrogen Inorganic materials 0.000 claims 9
- 239000000651 prodrug Chemical group 0.000 claims 9
- 229940002612 prodrug Drugs 0.000 claims 9
- 125000006620 amino-(C1-C6) alkyl group Chemical group 0.000 claims 7
- 229910052799 carbon Inorganic materials 0.000 claims 7
- 229910052757 nitrogen Inorganic materials 0.000 claims 7
- 239000008194 pharmaceutical composition Substances 0.000 claims 7
- 229910052736 halogen Inorganic materials 0.000 claims 5
- 150000002367 halogens Chemical class 0.000 claims 5
- 125000001072 heteroaryl group Chemical group 0.000 claims 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 5
- 230000002265 prevention Effects 0.000 claims 5
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 5
- 150000001204 N-oxides Chemical group 0.000 claims 4
- 206010028980 Neoplasm Diseases 0.000 claims 4
- 208000008589 Obesity Diseases 0.000 claims 4
- 201000011510 cancer Diseases 0.000 claims 4
- 125000005842 heteroatom Chemical group 0.000 claims 4
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 4
- 235000020824 obesity Nutrition 0.000 claims 4
- 230000003287 optical effect Effects 0.000 claims 4
- 208000001072 type 2 diabetes mellitus Diseases 0.000 claims 4
- 206010006895 Cachexia Diseases 0.000 claims 3
- 208000032928 Dyslipidaemia Diseases 0.000 claims 3
- 208000030814 Eating disease Diseases 0.000 claims 3
- 208000019454 Feeding and Eating disease Diseases 0.000 claims 3
- 208000035150 Hypercholesterolemia Diseases 0.000 claims 3
- 208000031226 Hyperlipidaemia Diseases 0.000 claims 3
- 206010020772 Hypertension Diseases 0.000 claims 3
- 208000017170 Lipid metabolism disease Diseases 0.000 claims 3
- 102100026299 MAP kinase-interacting serine/threonine-protein kinase 1 Human genes 0.000 claims 3
- 101710139011 MAP kinase-interacting serine/threonine-protein kinase 1 Proteins 0.000 claims 3
- 102100033610 MAP kinase-interacting serine/threonine-protein kinase 2 Human genes 0.000 claims 3
- 101710138999 MAP kinase-interacting serine/threonine-protein kinase 2 Proteins 0.000 claims 3
- 125000000499 benzofuranyl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 claims 3
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 3
- 201000001883 cholelithiasis Diseases 0.000 claims 3
- 208000029078 coronary artery disease Diseases 0.000 claims 3
- 125000000753 cycloalkyl group Chemical group 0.000 claims 3
- 206010012601 diabetes mellitus Diseases 0.000 claims 3
- 235000014632 disordered eating Nutrition 0.000 claims 3
- 230000000694 effects Effects 0.000 claims 3
- 208000001130 gallstones Diseases 0.000 claims 3
- 125000004464 hydroxyphenyl group Chemical group 0.000 claims 3
- 201000001421 hyperglycemia Diseases 0.000 claims 3
- 125000001041 indolyl group Chemical group 0.000 claims 3
- 230000004968 inflammatory condition Effects 0.000 claims 3
- 208000015122 neurodegenerative disease Diseases 0.000 claims 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 3
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 3
- 201000008482 osteoarthritis Diseases 0.000 claims 3
- 229910052760 oxygen Inorganic materials 0.000 claims 3
- 125000004307 pyrazin-2-yl group Chemical group [H]C1=C([H])N=C(*)C([H])=N1 0.000 claims 3
- 201000002859 sleep apnea Diseases 0.000 claims 3
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims 2
- PNZKKQWBSPXAPD-UHFFFAOYSA-N 4-[[6-(1h-indol-2-yl)pyrazin-2-yl]amino]-3-methoxy-n-methyl-n-(1-methylpyrrolidin-3-yl)benzamide Chemical compound C=1C=C(NC=2N=C(C=NC=2)C=2NC3=CC=CC=C3C=2)C(OC)=CC=1C(=O)N(C)C1CCN(C)C1 PNZKKQWBSPXAPD-UHFFFAOYSA-N 0.000 claims 2
- 125000004195 4-methylpiperazin-1-yl group Chemical group [H]C([H])([H])N1C([H])([H])C([H])([H])N(*)C([H])([H])C1([H])[H] 0.000 claims 2
- VEFWZQFPBUSMBL-UHFFFAOYSA-N [4-[[6-(1h-indol-2-yl)pyrazin-2-yl]amino]-3-methoxyphenyl]-morpholin-4-ylmethanone Chemical compound C=1C=C(NC=2N=C(C=NC=2)C=2NC3=CC=CC=C3C=2)C(OC)=CC=1C(=O)N1CCOCC1 VEFWZQFPBUSMBL-UHFFFAOYSA-N 0.000 claims 2
- 125000002252 acyl group Chemical group 0.000 claims 2
- 150000001412 amines Chemical class 0.000 claims 2
- 125000004391 aryl sulfonyl group Chemical group 0.000 claims 2
- 125000005334 azaindolyl group Chemical group N1N=C(C2=CC=CC=C12)* 0.000 claims 2
- 125000004196 benzothienyl group Chemical group S1C(=CC2=C1C=CC=C2)* 0.000 claims 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 2
- 208000035475 disorder Diseases 0.000 claims 2
- 125000005223 heteroarylcarbonyl group Chemical group 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- 239000000825 pharmaceutical preparation Substances 0.000 claims 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
- 125000000168 pyrrolyl group Chemical group 0.000 claims 2
- 229910052717 sulfur Inorganic materials 0.000 claims 2
- 125000001544 thienyl group Chemical group 0.000 claims 2
- IPBNVTMTIKJPSK-UHFFFAOYSA-N (3-aminoazetidin-1-yl)-[4-[[6-(5-fluoro-1h-indol-2-yl)pyrazin-2-yl]amino]-3-methoxyphenyl]methanone Chemical compound C=1C=C(NC=2N=C(C=NC=2)C=2NC3=CC=C(F)C=C3C=2)C(OC)=CC=1C(=O)N1CC(N)C1 IPBNVTMTIKJPSK-UHFFFAOYSA-N 0.000 claims 1
- NCJJBSPRMXVTIW-UHFFFAOYSA-N (4-ethylpiperazin-1-yl)-[4-[[6-(1h-indol-2-yl)pyrazin-2-yl]amino]-3-methoxyphenyl]methanone Chemical compound C1CN(CC)CCN1C(=O)C(C=C1OC)=CC=C1NC1=CN=CC(C=2NC3=CC=CC=C3C=2)=N1 NCJJBSPRMXVTIW-UHFFFAOYSA-N 0.000 claims 1
- JNQRUUBGEMDSNI-UHFFFAOYSA-N (4-ethylpiperazin-1-yl)-[6-[[6-(1h-indol-2-yl)pyrazin-2-yl]amino]pyridin-3-yl]methanone Chemical compound C1CN(CC)CCN1C(=O)C(C=N1)=CC=C1NC1=CN=CC(C=2NC3=CC=CC=C3C=2)=N1 JNQRUUBGEMDSNI-UHFFFAOYSA-N 0.000 claims 1
- XITUAKFNJMJXQZ-UHFFFAOYSA-N (4-methyl-1,4-diazepan-1-yl)-[6-[[6-(1h-pyrrolo[3,2-c]pyridin-2-yl)pyrazin-2-yl]amino]pyridin-3-yl]methanone Chemical compound C1CN(C)CCCN1C(=O)C(C=N1)=CC=C1NC1=CN=CC(C=2NC3=CC=NC=C3C=2)=N1 XITUAKFNJMJXQZ-UHFFFAOYSA-N 0.000 claims 1
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims 1
- 125000006704 (C5-C6) cycloalkyl group Chemical group 0.000 claims 1
- XCUZPVBDBASDCD-UHFFFAOYSA-N 2,9-diazaspiro[4.5]decan-2-yl-[4-[[6-(1h-indol-2-yl)pyrazin-2-yl]amino]-3-methoxyphenyl]methanone Chemical compound C=1C=C(NC=2N=C(C=NC=2)C=2NC3=CC=CC=C3C=2)C(OC)=CC=1C(=O)N(C1)CCC21CCCNC2 XCUZPVBDBASDCD-UHFFFAOYSA-N 0.000 claims 1
- PHLZSOMVNDLFQN-UHFFFAOYSA-N 2-[2-[[6-(5-fluoro-1h-indol-2-yl)pyrazin-2-yl]amino]-5-(4-methylpiperazine-1-carbonyl)phenoxy]-n,n-dimethylacetamide Chemical compound C=1C=C(NC=2N=C(C=NC=2)C=2NC3=CC=C(F)C=C3C=2)C(OCC(=O)N(C)C)=CC=1C(=O)N1CCN(C)CC1 PHLZSOMVNDLFQN-UHFFFAOYSA-N 0.000 claims 1
- GMDXKZWRGGYIIL-UHFFFAOYSA-N 2-[6-[4-(4-methylpiperazine-1-carbonyl)anilino]pyrazin-2-yl]-1h-indole-5-carboxamide Chemical compound C1CN(C)CCN1C(=O)C(C=C1)=CC=C1NC1=CN=CC(C=2NC3=CC=C(C=C3C=2)C(N)=O)=N1 GMDXKZWRGGYIIL-UHFFFAOYSA-N 0.000 claims 1
- FUJKGZVXJCWRRN-UHFFFAOYSA-N 3-(1h-indol-2-yl)pyrazin-2-amine Chemical compound NC1=NC=CN=C1C1=CC2=CC=CC=C2N1 FUJKGZVXJCWRRN-UHFFFAOYSA-N 0.000 claims 1
- DPHUNMBXCBPBOC-UHFFFAOYSA-N 3-[[6-(1-benzofuran-2-yl)pyrazin-2-yl]amino]-4-methoxy-n-methyl-n-(1-methylpyrrolidin-3-yl)benzamide Chemical compound C1=C(NC=2N=C(C=NC=2)C=2OC3=CC=CC=C3C=2)C(OC)=CC=C1C(=O)N(C)C1CCN(C)C1 DPHUNMBXCBPBOC-UHFFFAOYSA-N 0.000 claims 1
- ZHRBUSCAJPHBJY-UHFFFAOYSA-N 3-chloro-n-[2-(diethylamino)ethyl]-4-[[6-(5-fluoro-1h-indol-2-yl)pyrazin-2-yl]amino]benzamide Chemical compound ClC1=CC(C(=O)NCCN(CC)CC)=CC=C1NC1=CN=CC(C=2NC3=CC=C(F)C=C3C=2)=N1 ZHRBUSCAJPHBJY-UHFFFAOYSA-N 0.000 claims 1
- ANESEZVJTLJYQN-UHFFFAOYSA-N 3-fluoro-4-[6-(6-fluoro-1h-indol-2-yl)pyrazin-2-yl]-n-methyl-n-(1-methylpyrrolidin-3-yl)benzamide Chemical compound C=1C=C(C=2N=C(C=NC=2)C=2NC3=CC(F)=CC=C3C=2)C(F)=CC=1C(=O)N(C)C1CCN(C)C1 ANESEZVJTLJYQN-UHFFFAOYSA-N 0.000 claims 1
- PKUBWSRLUOHNPZ-UHFFFAOYSA-N 3-fluoro-5-[6-(6-fluoro-1h-indol-2-yl)pyrazin-2-yl]-n-methyl-n-(1-methylpyrrolidin-3-yl)benzamide Chemical compound C=1C(F)=CC(C=2N=C(C=NC=2)C=2NC3=CC(F)=CC=C3C=2)=CC=1C(=O)N(C)C1CCN(C)C1 PKUBWSRLUOHNPZ-UHFFFAOYSA-N 0.000 claims 1
- RZLKZEGKUUMPDQ-UHFFFAOYSA-N 3-methoxy-4-[[6-(4-methoxy-1h-indol-2-yl)pyrazin-2-yl]amino]-n-methyl-n-(1-methylpyrrolidin-3-yl)benzamide Chemical compound C=1C=C(NC=2N=C(C=NC=2)C=2NC3=CC=CC(OC)=C3C=2)C(OC)=CC=1C(=O)N(C)C1CCN(C)C1 RZLKZEGKUUMPDQ-UHFFFAOYSA-N 0.000 claims 1
- OVSTYTDVQDWUBE-UHFFFAOYSA-N 3-methoxy-4-[[6-(5-methoxy-1h-indol-2-yl)pyrazin-2-yl]amino]-n-methyl-n-(1-methylpyrrolidin-3-yl)benzamide Chemical compound C=1C2=CC(OC)=CC=C2NC=1C(N=1)=CN=CC=1NC(C(=C1)OC)=CC=C1C(=O)N(C)C1CCN(C)C1 OVSTYTDVQDWUBE-UHFFFAOYSA-N 0.000 claims 1
- UNUXUUBNCRXUMH-UHFFFAOYSA-N 3-methoxy-n-methyl-4-[[6-(5-methyl-1h-indol-2-yl)pyrazin-2-yl]amino]-n-(1-methylpyrrolidin-3-yl)benzamide Chemical compound C=1C=C(NC=2N=C(C=NC=2)C=2NC3=CC=C(C)C=C3C=2)C(OC)=CC=1C(=O)N(C)C1CCN(C)C1 UNUXUUBNCRXUMH-UHFFFAOYSA-N 0.000 claims 1
- XMTXOOYCGUDHQX-UHFFFAOYSA-N 3-methoxy-n-methyl-4-[[6-(6-methyl-1h-indol-2-yl)pyrazin-2-yl]amino]-n-(1-methylpyrrolidin-3-yl)benzamide Chemical compound C=1C=C(NC=2N=C(C=NC=2)C=2NC3=CC(C)=CC=C3C=2)C(OC)=CC=1C(=O)N(C)C1CCN(C)C1 XMTXOOYCGUDHQX-UHFFFAOYSA-N 0.000 claims 1
- OGSUUHVBRCGZAU-UHFFFAOYSA-N 4-[5-amino-6-(1-benzofuran-2-yl)pyrazin-2-yl]-n-(2,3-dihydroxypropyl)benzamide Chemical compound N1=C(C=2OC3=CC=CC=C3C=2)C(N)=NC=C1C1=CC=C(C(=O)NCC(O)CO)C=C1 OGSUUHVBRCGZAU-UHFFFAOYSA-N 0.000 claims 1
- OGSUUHVBRCGZAU-INIZCTEOSA-N 4-[5-amino-6-(1-benzofuran-2-yl)pyrazin-2-yl]-n-[(2s)-2,3-dihydroxypropyl]benzamide Chemical compound N1=C(C=2OC3=CC=CC=C3C=2)C(N)=NC=C1C1=CC=C(C(=O)NC[C@H](O)CO)C=C1 OGSUUHVBRCGZAU-INIZCTEOSA-N 0.000 claims 1
- HJANIWAXHMBUSG-UHFFFAOYSA-N 4-[5-amino-6-(1-benzofuran-2-yl)pyrazin-2-yl]-n-[3-[bis(2-hydroxyethyl)amino]propyl]benzamide Chemical compound N1=C(C=2OC3=CC=CC=C3C=2)C(N)=NC=C1C1=CC=C(C(=O)NCCCN(CCO)CCO)C=C1 HJANIWAXHMBUSG-UHFFFAOYSA-N 0.000 claims 1
- LANXWFYAJDTUQO-UHFFFAOYSA-N 4-[5-amino-6-(1-benzofuran-2-yl)pyrazin-2-yl]-n-ethyl-n-(2-hydroxyethyl)benzamide Chemical compound C1=CC(C(=O)N(CCO)CC)=CC=C1C1=CN=C(N)C(C=2OC3=CC=CC=C3C=2)=N1 LANXWFYAJDTUQO-UHFFFAOYSA-N 0.000 claims 1
- FANHFMGLTLDNKK-UHFFFAOYSA-N 4-[[6-(1-benzofuran-2-yl)pyrazin-2-yl]amino]-3-methoxy-n-methyl-n-(1-methylpyrrolidin-3-yl)benzamide Chemical compound C=1C=C(NC=2N=C(C=NC=2)C=2OC3=CC=CC=C3C=2)C(OC)=CC=1C(=O)N(C)C1CCN(C)C1 FANHFMGLTLDNKK-UHFFFAOYSA-N 0.000 claims 1
- YDYGKLHXQAFPOD-QGZVFWFLSA-N 4-[[6-(1h-indol-2-yl)pyrazin-2-yl]amino]-3-methoxy-n-[(3r)-pyrrolidin-3-yl]benzamide Chemical compound C=1C=C(NC=2N=C(C=NC=2)C=2NC3=CC=CC=C3C=2)C(OC)=CC=1C(=O)N[C@@H]1CCNC1 YDYGKLHXQAFPOD-QGZVFWFLSA-N 0.000 claims 1
- YDYGKLHXQAFPOD-KRWDZBQOSA-N 4-[[6-(1h-indol-2-yl)pyrazin-2-yl]amino]-3-methoxy-n-[(3s)-pyrrolidin-3-yl]benzamide Chemical compound C=1C=C(NC=2N=C(C=NC=2)C=2NC3=CC=CC=C3C=2)C(OC)=CC=1C(=O)N[C@H]1CCNC1 YDYGKLHXQAFPOD-KRWDZBQOSA-N 0.000 claims 1
- ZRZOSUIBWQOEGM-UHFFFAOYSA-N 4-[[6-(1h-indol-2-yl)pyrazin-2-yl]amino]-3-methoxy-n-piperidin-3-ylbenzamide Chemical compound C=1C=C(NC=2N=C(C=NC=2)C=2NC3=CC=CC=C3C=2)C(OC)=CC=1C(=O)NC1CCCNC1 ZRZOSUIBWQOEGM-UHFFFAOYSA-N 0.000 claims 1
- CGPRHVRLWRCWJA-UHFFFAOYSA-N 4-[[6-(4-fluoro-1h-indol-2-yl)pyrazin-2-yl]amino]-3-methoxy-n-methyl-n-(1-methylpyrrolidin-3-yl)benzamide Chemical compound C=1C=C(NC=2N=C(C=NC=2)C=2NC3=CC=CC(F)=C3C=2)C(OC)=CC=1C(=O)N(C)C1CCN(C)C1 CGPRHVRLWRCWJA-UHFFFAOYSA-N 0.000 claims 1
- ZJPPAUXADIFCJC-UHFFFAOYSA-N 4-[[6-(5-chloro-1h-indol-2-yl)pyrazin-2-yl]amino]-3-methoxy-n-methyl-n-(1-methylpyrrolidin-3-yl)benzamide Chemical compound C=1C=C(NC=2N=C(C=NC=2)C=2NC3=CC=C(Cl)C=C3C=2)C(OC)=CC=1C(=O)N(C)C1CCN(C)C1 ZJPPAUXADIFCJC-UHFFFAOYSA-N 0.000 claims 1
- PLYJSWZGCPGSCQ-UHFFFAOYSA-N 4-[[6-(5-cyano-1h-indol-2-yl)pyrazin-2-yl]amino]-3-methoxy-n-methyl-n-(1-methylpyrrolidin-3-yl)benzamide Chemical compound C=1C=C(NC=2N=C(C=NC=2)C=2NC3=CC=C(C=C3C=2)C#N)C(OC)=CC=1C(=O)N(C)C1CCN(C)C1 PLYJSWZGCPGSCQ-UHFFFAOYSA-N 0.000 claims 1
- NWLPGLSOMDEYCD-UHFFFAOYSA-N 4-[[6-(5-fluoro-1h-indol-2-yl)pyrazin-2-yl]amino]-3-methoxy-n-methyl-n-(1-methylpyrrolidin-3-yl)benzamide Chemical compound C=1C=C(NC=2N=C(C=NC=2)C=2NC3=CC=C(F)C=C3C=2)C(OC)=CC=1C(=O)N(C)C1CCN(C)C1 NWLPGLSOMDEYCD-UHFFFAOYSA-N 0.000 claims 1
- GBTXJILKTQBTQO-UHFFFAOYSA-N 4-[[6-(6-chloro-1h-indol-2-yl)pyrazin-2-yl]amino]-3-methoxy-n-methyl-n-(1-methylpyrrolidin-3-yl)benzamide Chemical compound C=1C=C(NC=2N=C(C=NC=2)C=2NC3=CC(Cl)=CC=C3C=2)C(OC)=CC=1C(=O)N(C)C1CCN(C)C1 GBTXJILKTQBTQO-UHFFFAOYSA-N 0.000 claims 1
- KFNNXOYZKPSREJ-UHFFFAOYSA-N 4-[[6-(6-fluoro-1h-indol-2-yl)pyrazin-2-yl]amino]-3-methoxy-n-methyl-n-(1-methylpyrrolidin-3-yl)benzamide Chemical compound C=1C=C(NC=2N=C(C=NC=2)C=2NC3=CC(F)=CC=C3C=2)C(OC)=CC=1C(=O)N(C)C1CCN(C)C1 KFNNXOYZKPSREJ-UHFFFAOYSA-N 0.000 claims 1
- QDBWBNDBUKEGSC-UHFFFAOYSA-N 4-[[6-(7-fluoro-1h-indol-2-yl)pyrazin-2-yl]amino]-3-methoxy-n-methyl-n-(1-methylpyrrolidin-3-yl)benzamide Chemical compound C=1C=C(NC=2N=C(C=NC=2)C=2NC3=C(F)C=CC=C3C=2)C(OC)=CC=1C(=O)N(C)C1CCN(C)C1 QDBWBNDBUKEGSC-UHFFFAOYSA-N 0.000 claims 1
- RCOTZFFXLPZDMS-GOSISDBHSA-N [(3r)-3-(dimethylamino)pyrrolidin-1-yl]-[3-methoxy-4-[[6-(1h-pyrrolo[3,2-c]pyridin-2-yl)pyrazin-2-yl]amino]phenyl]methanone Chemical compound C=1C=C(NC=2N=C(C=NC=2)C=2NC3=CC=NC=C3C=2)C(OC)=CC=1C(=O)N1CC[C@@H](N(C)C)C1 RCOTZFFXLPZDMS-GOSISDBHSA-N 0.000 claims 1
- AHAWPPZIBXCDSQ-HXUWFJFHSA-N [(3r)-3-(dimethylamino)pyrrolidin-1-yl]-[4-[[6-(1h-indol-2-yl)pyrazin-2-yl]amino]phenyl]methanone Chemical compound C1[C@H](N(C)C)CCN1C(=O)C(C=C1)=CC=C1NC1=CN=CC(C=2NC3=CC=CC=C3C=2)=N1 AHAWPPZIBXCDSQ-HXUWFJFHSA-N 0.000 claims 1
- YSJOQWCLLYPLTQ-QGZVFWFLSA-N [(3r)-3-aminopyrrolidin-1-yl]-[4-[[6-(1h-indol-2-yl)pyrazin-2-yl]amino]-3-methoxyphenyl]methanone Chemical compound C=1C=C(NC=2N=C(C=NC=2)C=2NC3=CC=CC=C3C=2)C(OC)=CC=1C(=O)N1CC[C@@H](N)C1 YSJOQWCLLYPLTQ-QGZVFWFLSA-N 0.000 claims 1
- ONYIMVNCXQKHJT-QGZVFWFLSA-N [(3r)-3-aminopyrrolidin-1-yl]-[4-[[6-(5-fluoro-1h-indol-2-yl)pyrazin-2-yl]amino]-3-methoxyphenyl]methanone Chemical compound C=1C=C(NC=2N=C(C=NC=2)C=2NC3=CC=C(F)C=C3C=2)C(OC)=CC=1C(=O)N1CC[C@@H](N)C1 ONYIMVNCXQKHJT-QGZVFWFLSA-N 0.000 claims 1
- XLWQOGPOLMFUFI-CALCHBBNSA-N [(3r,5s)-3,5-dimethylpiperazin-1-yl]-[4-[[6-(1h-indol-2-yl)pyrazin-2-yl]amino]-3-methoxyphenyl]methanone Chemical compound C=1C=C(NC=2N=C(C=NC=2)C=2NC3=CC=CC=C3C=2)C(OC)=CC=1C(=O)N1C[C@H](C)N[C@H](C)C1 XLWQOGPOLMFUFI-CALCHBBNSA-N 0.000 claims 1
- AHAWPPZIBXCDSQ-FQEVSTJZSA-N [(3s)-3-(dimethylamino)pyrrolidin-1-yl]-[4-[[6-(1h-indol-2-yl)pyrazin-2-yl]amino]phenyl]methanone Chemical compound C1[C@@H](N(C)C)CCN1C(=O)C(C=C1)=CC=C1NC1=CN=CC(C=2NC3=CC=CC=C3C=2)=N1 AHAWPPZIBXCDSQ-FQEVSTJZSA-N 0.000 claims 1
- YSJOQWCLLYPLTQ-KRWDZBQOSA-N [(3s)-3-aminopyrrolidin-1-yl]-[4-[[6-(1h-indol-2-yl)pyrazin-2-yl]amino]-3-methoxyphenyl]methanone Chemical compound C=1C=C(NC=2N=C(C=NC=2)C=2NC3=CC=CC=C3C=2)C(OC)=CC=1C(=O)N1CC[C@H](N)C1 YSJOQWCLLYPLTQ-KRWDZBQOSA-N 0.000 claims 1
- MEQAZNGFRKGLQN-UHFFFAOYSA-N [2-chloro-4-[[6-(1h-indol-2-yl)pyrazin-2-yl]amino]phenyl]-piperazin-1-ylmethanone Chemical compound ClC1=CC(NC=2N=C(C=NC=2)C=2NC3=CC=CC=C3C=2)=CC=C1C(=O)N1CCNCC1 MEQAZNGFRKGLQN-UHFFFAOYSA-N 0.000 claims 1
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- ULIMCJSUTRFRIF-UHFFFAOYSA-N n-[2-(diethylamino)ethyl]-2-fluoro-4-[[6-(1h-indol-2-yl)pyrazin-2-yl]amino]benzamide Chemical compound C1=C(F)C(C(=O)NCCN(CC)CC)=CC=C1NC1=CN=CC(C=2NC3=CC=CC=C3C=2)=N1 ULIMCJSUTRFRIF-UHFFFAOYSA-N 0.000 claims 1
- QFDRBXUQNMKNAH-UHFFFAOYSA-N n-[2-(diethylamino)ethyl]-4-[5-(1h-indol-2-yl)pyridin-3-yl]benzamide Chemical compound C1=CC(C(=O)NCCN(CC)CC)=CC=C1C1=CN=CC(C=2NC3=CC=CC=C3C=2)=C1 QFDRBXUQNMKNAH-UHFFFAOYSA-N 0.000 claims 1
- GLWMBNCIIMAGKE-UHFFFAOYSA-N n-[2-(diethylamino)ethyl]-4-[[6-(1h-indol-2-yl)pyrazin-2-yl]amino]-3-methoxybenzamide Chemical compound COC1=CC(C(=O)NCCN(CC)CC)=CC=C1NC1=CN=CC(C=2NC3=CC=CC=C3C=2)=N1 GLWMBNCIIMAGKE-UHFFFAOYSA-N 0.000 claims 1
- TUNJGJAVESBYRU-UHFFFAOYSA-N n-[2-(diethylamino)ethyl]-4-[[6-(5-fluoro-1h-indol-2-yl)pyrazin-2-yl]amino]-3-methoxybenzamide Chemical compound COC1=CC(C(=O)NCCN(CC)CC)=CC=C1NC1=CN=CC(C=2NC3=CC=C(F)C=C3C=2)=N1 TUNJGJAVESBYRU-UHFFFAOYSA-N 0.000 claims 1
- QEHZTXHMFSBBQW-UHFFFAOYSA-N n-[2-(dimethylamino)ethyl]-4-[[6-(1h-indol-2-yl)pyrazin-2-yl]amino]-3-methoxy-n-methylbenzamide Chemical compound COC1=CC(C(=O)N(C)CCN(C)C)=CC=C1NC1=CN=CC(C=2NC3=CC=CC=C3C=2)=N1 QEHZTXHMFSBBQW-UHFFFAOYSA-N 0.000 claims 1
- JWJMWQRKAQBITG-UHFFFAOYSA-N n-[3-(dimethylamino)propyl]-4-[6-(1h-indol-2-yl)pyrazin-2-yl]-n-methylbenzamide Chemical compound C1=CC(C(=O)N(C)CCCN(C)C)=CC=C1C1=CN=CC(C=2NC3=CC=CC=C3C=2)=N1 JWJMWQRKAQBITG-UHFFFAOYSA-N 0.000 claims 1
- VTNHHYGXQQBHGX-UHFFFAOYSA-N n-[3-(dimethylamino)propyl]-4-[[6-(1h-indol-2-yl)pyrazin-2-yl]amino]-3-methoxybenzamide Chemical compound COC1=CC(C(=O)NCCCN(C)C)=CC=C1NC1=CN=CC(C=2NC3=CC=CC=C3C=2)=N1 VTNHHYGXQQBHGX-UHFFFAOYSA-N 0.000 claims 1
- KRAFXUXYGUZYOZ-UHFFFAOYSA-N n-ethyl-n-(2-hydroxyethyl)-4-[6-(1h-indol-2-yl)pyrazin-2-yl]benzamide Chemical compound C1=CC(C(=O)N(CCO)CC)=CC=C1C1=CN=CC(C=2NC3=CC=CC=C3C=2)=N1 KRAFXUXYGUZYOZ-UHFFFAOYSA-N 0.000 claims 1
- DNUTZBZXLPWRJG-UHFFFAOYSA-M piperidine-1-carboxylate Chemical compound [O-]C(=O)N1CCCCC1 DNUTZBZXLPWRJG-UHFFFAOYSA-M 0.000 claims 1
- 125000003107 substituted aryl group Chemical group 0.000 claims 1
- 208000024891 symptom Diseases 0.000 claims 1
- 238000002560 therapeutic procedure Methods 0.000 claims 1
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| US5430123A (en) * | 1994-02-04 | 1995-07-04 | Hoechst Celanese Corporation | Polymer compositions containing substituted pyrazines |
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2007
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- 2007-06-21 ES ES07786791T patent/ES2340093T3/es active Active
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- 2007-06-21 CA CA002654358A patent/CA2654358A1/en not_active Abandoned
- 2007-06-21 BR BRPI0713328-6A patent/BRPI0713328A2/pt not_active IP Right Cessation
- 2007-06-21 RU RU2009101911/04A patent/RU2009101911A/ru not_active Application Discontinuation
- 2007-06-21 US US11/821,565 patent/US20080039450A1/en not_active Abandoned
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- 2007-06-21 AT AT07786791T patent/ATE456565T1/de not_active IP Right Cessation
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